BEUDAMED
    FDA Adverse Event Summary report: N

    ALWAYS

    MDR report key: 526515 · Received April 28, 2004

    Report

    Report Number
    MW4003712
    Date Received
    April 28, 2004
    Report Date
    January 29, 2004
    Manufacturer
    *
    Product Code
    HHL
    Report Source
    Voluntary report
    Reporter Location
    FL, US
    Reporter Occupation
    PATIENT

    Narratives

    Description of Event or Problem · 1

    THE COMPLAINANT PURCHASED A 24 PACKAGE OF ALWAYS MAXI-PADS AT NONE GROCERY STORE. THEY USED APPROX 10 PADS AND WHEN GOING TO GET ANOTHER PAD FROM THE PLASTIC CONTAINER; THEY SAW A SYRINGE/NEEDLE INSIDE THE PACKAGE. THE COMPLAINANT CONTACTED THE SHERIFF'S DEPARTMENT AND SPOKE WITH DEPUTY. DEPUTY COLLECTED THE NEEDLE, THE PACKAGING, AND THE RECEIPT FOR THE PURCHASE.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 ALWAYS MAXI-PADS HHL * * *

    Patients

    Seq Age Sex Outcome Treatment
    1 *